Allele Registry

Canonical Allele Identifier: PA2826625317

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000568421

RCV002528146

RCV004001068

ClinVar Variation:

483888

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ser211Cys	CA067038 NM_001281492.2:c.632C>G